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Severe Paediatric Disorders v0.12 | UGT1A1 | Louise Daugherty reviewed gene: UGT1A1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.11 | UGT1A1 | Louise Daugherty Publications for gene UGT1A1 were updated from to 30847515 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.10 | UGT1A1 | Louise Daugherty Added phenotypes Crigler-Najjar syndrome, type I, 218800; Crigler-Najjar syndrome, type II, 606785; Hyperbilirubinemia, familial transient neonatal, 237900 for gene: UGT1A1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.9 | UGT1A1 | Louise Daugherty Added phenotypes Crigler-Najjar syndrome, type I, 218800; Crigler-Najjar syndrome, type II, 606785; Hyperbilirubinemia, familial transient neonatal, 237900 for gene: UGT1A1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.9 | UGT1A1 | Louise Daugherty Added phenotypes Crigler-Najjar syndrome, type I, 218800; Crigler-Najjar syndrome, type II, 606785; Hyperbilirubinemia, familial transient neonatal, 237900 for gene: UGT1A1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.8 | UGT1A1 | Louise Daugherty Added phenotypes Hyperbilirubinemia, familial transient neonatal, 237900; Crigler-Najjar syndrome, type II, 606785; Crigler-Najjar syndrome, type I, 218800 for gene: UGT1A1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.8 | UGT1A1 |
Louise Daugherty Mode of inheritance for gene UGT1A1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Crigler-Najjar syndrome, type I, 218800; Crigler-Najjar syndrome, type II, 606785; Hyperbilirubinemia, familial transient neonatal, 237900 for gene: UGT1A1 |
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Severe Paediatric Disorders v0.7 | UGT1A1 | Louise Daugherty Source Next Generation Children Project was added to UGT1A1. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Severe Paediatric Disorders v0.5 | UGT1A1 |
Louise Daugherty Source Expert Review Green was added to UGT1A1. Rating Changed from Red List (low evidence) to Green List (high evidence) |
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Severe Paediatric Disorders v0.4 | UGT1A1 |
Louise Daugherty gene: UGT1A1 was added gene: UGT1A1 was added to Severe Paediatric Disorders. Sources: Expert list Mode of inheritance for gene: UGT1A1 was set to |